26509-49-9

Upstream product

• 26509-47-7 2,6-diallyl-4-methylphenol 
• 5397-51-3 allyl-(4-methyl-2,6-dipropyl-phenyl)-ether 
• 1121-70-6 sodium 4-methylphenoxide 
• 6628-06-4 2-allyl-4-methylphenol 
• 71-23-8 propan-1-ol 
• 106-44-5 p-cresol 
• 51496-25-4 3-allyl-4-allyloxytoluene 
• 854260-67-6 allyl-(4-methyl-2-propyl-phenyl)-ether 
• 4074-46-8 2-propyl-4-methylphenol 
• 23431-48-3 allyl p-tolyl ether 
• 26509-48-8 4-Hydroxy-1-methyl-5-propyl-3-allyl-benzol 

Downstream Products

• 5397-51-3 allyl-(4-methyl-2,6-dipropyl-phenyl)-ether 

Relevant academic research and scientific papers

": A Jack of Trio "-robust one-pot metal free oxidative amination, azidation and peroxidation of phenols

Herein we disclose a highly efficient methodology for the generation of nitrogen containing quaternary carbon centres via aminative and azidative oxidative dearomatization of phenols. The same protocol has also been successfully employed to achieve oxidative peroxidation of phenols. The simplest metal free reaction conditions delineate an easy breakthrough to the "Trio"- oxidative amination, azidation and peroxidation. An array of diverse polyfunctionalised heterocycles has been synthesized in one pot.

Catalytic alkylation of cresols with propanol-1

Study of the reaction of alkylation of ortho-, meta-, and para-cresols with propanol-1 in the presence of ferrite cobalt and manganese catalysts is reported. The effect of the catalyst composition and reaction conditions on the yield and isomeric composit